Koby Surgical
Country not established
- Devices
- 1
What Koby Surgical makes
Koby Surgical manufactures the KOBY SURGICAL INTERNAL FIXATION SYSTEM, a device used for orthopedic internal fixation to stabilize bone fractures or surgical repairs.
The company’s portfolio is regulated under FDA Class II devices, with the KOBY SURGICAL INTERNAL FIXATION SYSTEM listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Koby Surgical Internal Fixation System Ref K060026
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Koby Surgical have in the registry?
The registry currently lists 1 device for Koby Surgical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Koby Surgical's devices?
Among its 1 most recently registered device, Koby Surgical has devices listed in FDA 510(k) (1 device).
What risk classes do Koby Surgical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Koby Surgical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Koby Surgical in the registry?
The most recently registered devices listed for Koby Surgical include KOBY SURGICAL INTERNAL FIXATION SYSTEM.